466 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Monitor, Uterine Contraction, External (For Use In Clinic)
FDA Pre-Market Approval
FDA Class 2
·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.
MSI 2002 SERIES BED
FDA 510(k)
FDA Class 2
·General Hospital
MSI 9000 SERIES BED
FDA 510(k)
FDA Class 2
·General Hospital
MSI 3002 SERIES BED
FDA 510(k)
FDA Class 2
·General Hospital
MSI STANDARD BED MODELS L1098-84/L1098-74/L1085-74
FDA 510(k)
FDA Class 2
·General Hospital
MSI 5000 SERIES BED
FDA 510(k)
FDA Class 2
·General Hospital
MSI 4000 SERIES BED
FDA 510(k)
FDA Class 2
·General Hospital
DISPOSABLE INJECTION NEEDLE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Vitavitro Vitrification Kit, Vitavitro Warming Kit, and Vitavitro Straw Set
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
VitaVitro® Single Lumen Oocyte Retrieval Needle (ORNS-17G, ORNS-18G), VitaVitro® Double Lumen Oocyte Retrieval Needle (ORND-17G)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
System, Test, Carcinoembryonic Antigen
FDA Pre-Market Approval
FDA Class 2
·CEA-ROCHE(R) EIA
TinniLogic Mobile Tinnitus Management Device
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Zirdent Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank
FDA 510(k)
FDA Class 2
·Dental
PANTHEON SPINAL IBFD SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic